Abstract

Human umbilical cord perivascular cells (HUCPVCs), harvested from human umbilical cord perivascular tissue, show potential for future use as an alternative to mesenchymal stromal cells. Here, we present the results for the characterization of the properties alkaline phosphatase-positive HUCPVCs (ALP(+)-HUCPVCs). These ALP(+)-HUCPVCs were created from HUCPVCs in this study by culturing in the presence of activated vitamin D3, an inhibitor of bone morphogenetic protein signaling and transforming growth factor-beta1 (TGF-β1). The morphological characteristics, cell proliferation, gene expression, and mineralization-inducing ability of ALP(+)-HUCPVCs were investigated at the morphological, biological, and genetic levels. ALP(+)-HUCPVCs possess high ALP gene expression and activity in cells and a slow rate of cell growth. The morphology of ALP(+)-HUCPVCs is fibroblast-like, with an increase in actin filaments containing alpha-smooth muscle actin. In addition to ALP expression, the gene expression levels of type I collagen, osteopontin, elastin, fibrillin-1, and cluster of differentiation 90 are increased in ALP(+)-HUCPVCs. ALP(+)-HUCPVCs do not have the ability to induce mineralization nodules, which may be due to the restriction of phosphate uptake into matrix vesicles. Moreover, ALP(+)-HUCPVCs may produce anti-mineralization substances. We conclude that ALP(+)-HUCPVCs induced from HUCPVCs by a TGF-β1 stimulation possess myofibroblast-like properties that have little mineralization-inducing ability.

Highlights

  • We first attempted to determine the optimum concentration for the differentiation of Human umbilical cord perivascular cells (HUCPVCs) into high alkaline phosphatase activity containing HUCPVCs (ALP(+)HUCPVCs) because the intrinsically high Alkaline Phosphatase (ALP) activity in cells is thought to affect cell growth [24]

  • Compared to the control cultured in the absence of vitamin D3 (VD), LDN, and TGF-β1, the ALP activity showed a tendency of increasing for the combination of VD and LDN or VD, LDN, and TGF-β1 on day 3

  • We decided to focus on HUCPVCs cultured in the presence of VD only (V-HUCPVCs); VD and LDN (VL-HUCPVCs); and VD, LDN, and TGF-β1 (ALP(+)-HUCPVCs) and found that LDN was a key factor for the differentiation of HUCPVCs to ALP(+)-HUCPVCs

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Summary

Introduction

Mesenchymal stem cells (MSCs) are a type of somatic stem cell derived from mesenchymal tissues such as bone marrow [1,2], the adipose tissue stromal vascular fraction [3,4], the placenta [5], and the umbilical cord [6,7]. MSCs possess self-replication and multilineage differentiation abilities and pose few risks for tumor formation, so they are expected to be a cell source for regenerative medicine. The MSCs isolated from each tissue have similar expression profiles and biological functions for cell surface markers but possess different characteristics depending on the tissues from which they were derived. Bone marrow MSCs have been widely used for both basic and clinic studies because of their ease of collection and high proliferative potential [2,8,9].

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